G. Puccio

发表

Role of TOMM40 rs10524523 polymorphism in onset of alzheimer's disease caused by the PSEN1 M146L mutation.

A. Bruni, M. Anfossi, L. Bernardi, 2013, Journal of Alzheimer's Disease.

A novel pathogenic PSEN1 mutation in a family with Alzheimer's disease: phenotypical and neuropathological features.

F. Tagliavini, A. Bruni, O. Bugiani, 2011, Journal of Alzheimer's disease : JAD.

PSEN1 and PRNP gene mutations: co-occurrence makes onset very early in a family with FTD phenotype.

A. Bruni, M. Anfossi, L. Bernardi, 2011, Journal of Alzheimer's disease : JAD.

The Genetic Variability of UCP4 Affects the Individual Susceptibility to Late-Onset Alzheimer's Disease and Modifies the Disease's Risk in APOE-ɛ4 Carriers.

A. Bruni, M. Anfossi, R. Maletta, 2016, Journal of Alzheimer's disease : JAD.

Novel N-terminal domain mutation in prion protein detected in 2 patients diagnosed with frontotemporal lobar degeneration syndrome

C. Cupidi, A. Bruni, M. Anfossi, 2014, Neurobiology of Aging.

Late onset familial Alzheimer's disease: novel presenilin 2 mutation and PS1 E318G polymorphism

A. Bruni, M. Anfossi, L. Bernardi, 2008, Journal of Neurology.

Presenilin 2 Ser130Leu mutation in a case of late-onset “sporadic” Alzheimer’s disease

A. Bruni, M. Anfossi, L. Bernardi, 2007, Journal of Neurology.

Neuropsychiatric or Behavioral and Psychological Symptoms of Dementia (BPSD): Focus on Prevalence and Natural History in Alzheimer's Disease and Frontotemporal Dementia

C. Cupidi, A. Bruni, F. Frangipane, 2022, Frontiers in Neurology.

Heterogeneity within a large kindred with frontotemporal dementia

J. Hardy, P. S. St George-Hyslop, A. Kertesz, 2007, Neurology.

A Novel Mutation (D395A) in Valosin-Containing Protein Gene Is Associated With Early Onset Frontotemporal Dementia in an Italian Family

A. Bruni, L. Bernardi, M. E. Conidi, 2021, Frontiers in Genetics.

The novel PSEN1 M84V mutation associated to frontal dysexecutive syndrome, spastic paraparesis, and cerebellar atrophy in a dominant Alzheimer's disease family

S. Sorbi, B. Nacmias, C. Cupidi, 2017, Neurobiology of Aging.

Prevalence of Delirium in a Population of Elderly Outpatients with Dementia: A Retrospective Study.

C. Cupidi, A. Bruni, F. Perticone, 2017, Journal of Alzheimer's disease : JAD.

Novel PSEN1 and PGRN mutations in early-onset familial frontotemporal dementia

A. Bruni, M. Anfossi, L. Bernardi, 2009, Neurobiology of Aging.

The effects of APOE and tau gene variability on risk of frontotemporal dementia

E. Rogaeva, T. Kawarai, L. Bernardi, 2006, Neurobiology of Aging.

Role of Niemann-Pick Type C Disease Mutations in Dementia.

C. Cupidi, A. Bruni, M. Anfossi, 2016, Journal of Alzheimer's disease : JAD.

Compound heterozygosity of 2 novel MAPT mutations in frontotemporal dementia

C. Duyckaerts, M. Spillantini, A. Bruni, 2011, Neurobiology of Aging.

Novel MAPT Val75Ala mutation and PSEN2 Arg62Hys in two siblings with frontotemporal dementia

A. Bruni, M. Anfossi, L. Bernardi, 2010, Neurological Sciences.

The first deep intronic mutation in the NOTCH3 gene in a family with late-onset CADASIL

A. Federico, M. Dotti, A. Bruni, 2013, Neurobiology of Aging.

Phenotypic expressions of Alzheimer’s disease: a gender perspective

C. Cupidi, A. Bruni, M. Anfossi, 2018 .

Worldwide distribution of PSEN1 Met146Leu mutation

S. Pappatà, S. Sorbi, G. Forloni, 2010, Neurology.

Homozygous carriers of APP A713T mutation in an autosomal dominant Alzheimer disease family

C. Cupidi, A. Bruni, M. Anfossi, 2015, Neurology.

Investigation of c9orf72 in 4 neurodegenerative disorders.

P. S. St George-Hyslop, R. Mayeux, L. Hazrati, 2012, Archives of neurology.

A Comparison of Behavioral and Psychological Symptoms of Dementia (BPSD) and BPSD Sub-Syndromes in Early-Onset and Late-Onset Alzheimer’s Disease

A. Bruni, F. Frangipane, R. Maletta, 2021, Journal of Alzheimer's disease : JAD.

Epidemiology and genetics of frontotemporal dementia: a door-to-door survey in Southern Italy

E. Rogaeva, P. George-Hyslop, C. Cupidi, 2012, Neurobiology of Aging.

A large Calabrian kindred segregating frontotemporal dementia

A. Paterson, T. Kawarai, A. Bruni, 2002, Journal of Neurology.

Amyloid Precursor Protein A713T Mutation in Calabrian Patients with Alzheimer’s Disease: A Population Genomics Approach to Estimate Inheritance from a Common Ancestor

C. van Broeckhoven, B. Borroni, C. Giuliani, 2021, Biomedicines.

Somatic comorbidities and Alzheimer’s disease treatment

A. Bruni, F. Frangipane, P. Gareri, 2013, Neurological Sciences.

Using the Theory of Planned Behavior and Past Behavior to Explain the Intention to Receive a Seasonal Influenza Vaccine among Family Caregivers of People with Dementia

A. Bruni, Paolo Abondio, F. Frangipane, 2023, International Journal of Translational Medicine.

Frequency of Cardiovascular Genetic Risk Factors in a Calabrian Population and Their Effects on Dementia.

C. Cupidi, A. Bruni, M. Anfossi, 2018, Journal of Alzheimer's disease : JAD.

AbetaPP A713T mutation in late onset Alzheimer's disease with cerebrovascular lesions.

A. Bruni, M. Anfossi, L. Bernardi, 2009, Journal of Alzheimer's disease : JAD.

MAPT V363I Variation in a Sporadic Case of Frontotemporal Dementia: Variable Penetrant Mutation or Rare Polymorphism?

A. Bruni, M. Anfossi, L. Bernardi, 2011, Alzheimer disease and associated disorders.